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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 94675

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
May 20, 2024
Product types
Drug
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Contract Pharmacal Corporation

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 1

Extra Strength Acetaminophen 500 MG Tablets,100-count Bottle, Distributed By: MAJOR PHARMACEUTICALS, 17177 N Laurel Park Drive, Suite 233, Livonia, MI USA 48152, NDC 0904-6730-60, UPC Number 309046730606

D-0566-2024
Recall number
D-0566-2024
Initiated
May 20, 2024
Classification
Class II
Status
Ongoing
Quantity
14,616 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Discoloration: Brownish tablets

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Discoloration: Brownish tablets

Code information

Lot#: 368638; Exp. 05/2025

Distribution pattern

MI